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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:168418

AF w/AS 550 x 0.5-7 ml,w/Y site,DL CPNB, Product code MVAXL2Y CPNB, Arrow AutoFuser Disposable Pain Control Pump

Official recall number

Z-0952-2019

Evidence summary

Product code
MEB
Recall status
Terminated
Event initiated
October 02, 2018
Root cause
Process control
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-0952-2019

Field note

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